In a prospective open study we evaluated whether intravenous dopamine
infusions can be safely switched to enterally administered ibopamine i
n dopamine-dependent patients. Six patients defined as being clinicall
y stable, normovolaemic, but dopamine dependent, i.e. with repeated in
ability to stop intravenous dopamine, were included. Ibopamine was adm
inistered via a nasogastric or nasoduodenal tube. During the initial 4
8-hour period of ibopamine administration the dopamine infusion was gr
adually decreased and then discontinued. Arterial blood pressure was c
ontinuously recorded via a 20-gauge cannula in the radial artery. Urin
e output was measured each hour. In all 6 patients it was possible to
decrease and then discontinue the dopamine infusion whilst maintaining
haemodynamic stability and an appropriate diuresis. It was then possi
ble to discharge the patients from the intensive care unit. Normovolae
mic, clinically stable but dopamine-dependent patients may be weaned o
ff intravenous dopamine by substitution of enterally administered ibop
amine, allowing discharge from the intensive care unit.